Variant report

Variant	rs2101150
Chromosome Location	chr5:113051354-113051355
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10035987	0.80[AMR][1000 genomes]
rs10478140	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10478141	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12521147	0.82[AMR][1000 genomes]
rs1482347	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1552156	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1552158	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1842760	0.84[AMR][1000 genomes]
rs1988077	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4705469	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4705470	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7734801	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113049200-113057400	Weak transcription	Fetal Kidney	kidney
2	chr5:113051000-113058200	Weak transcription	Fetal Lung	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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